Canonical Allele Identifier: CA377143379
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71709188A>C , CM000672.2:g.71709188A>C GRCh38
NC_000010.10:g.73468945A>C , CM000672.1:g.73468945A>C GRCh37
NC_000010.9:g.73138951A>C NCBI36
NG_008835.1:g.317242A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.3197A>C MANE Select ENSP00000224721.9:p.Tyr1066Ser
ENST00000398809.9:c.3197A>C ENSP00000381789.5:p.Tyr1066Ser
ENST00000442677.4:c.3197A>C ENSP00000388894.3:p.Tyr1066Ser
ENST00000466757.8:c.2628A>C
ENST00000224721.10:c.3212A>C ENSP00000224721.8:p.Tyr1071Ser
ENST00000398809.8:c.3197A>C ENSP00000381789.5:p.Tyr1066Ser
ENST00000442677.3:c.1972A>C
ENST00000466757.7:c.2628A>C
ENST00000616684.4:c.3197A>C ENSP00000482036.2:p.Tyr1066Ser
ENST00000622827.4:c.3197A>C ENSP00000483211.1:p.Tyr1066Ser
NM_001171930.1:c.3197A>C NP_001165401.1:p.Tyr1066Ser
NM_022124.5:c.3197A>C NP_071407.4:p.Tyr1066Ser
XM_006717940.2:c.3392A>C XP_006718003.1:p.Tyr1131Ser
XM_006717942.2:c.3326A>C XP_006718005.1:p.Tyr1109Ser
XM_011540039.1:c.3392A>C XP_011538341.1:p.Tyr1131Ser
XM_011540040.1:c.3386A>C XP_011538342.1:p.Tyr1129Ser
XM_011540041.1:c.3332A>C XP_011538343.1:p.Tyr1111Ser
XM_011540042.1:c.3392A>C XP_011538344.1:p.Tyr1131Ser
XM_011540043.1:c.3392A>C XP_011538345.1:p.Tyr1131Ser
XM_011540044.1:c.3257A>C XP_011538346.1:p.Tyr1086Ser
XM_011540045.1:c.3392A>C XP_011538347.1:p.Tyr1131Ser
XM_011540046.1:c.2852A>C XP_011538348.1:p.Tyr951Ser
XM_011540047.1:c.2210A>C XP_011538349.1:p.Tyr737Ser
XM_011540048.1:c.3392A>C XP_011538350.1:p.Tyr1131Ser
XM_011540049.1:c.3392A>C XP_011538351.1:p.Tyr1131Ser
XM_011540050.1:c.3392A>C XP_011538352.1:p.Tyr1131Ser
XM_011540051.1:c.3392A>C XP_011538353.1:p.Tyr1131Ser
XM_011540053.1:c.3392A>C XP_011538355.1:p.Tyr1131Ser
XR_945796.1:n.3635A>C
NM_001171930.2:c.3197A>C NP_001165401.1:p.Tyr1066Ser
NM_022124.6:c.3197A>C MANE Select NP_071407.4:p.Tyr1066Ser